Canonical Allele Identifier: CA2320568451

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714160T= , CM000681.2:g.6714160T=	GRCh38
NC_000019.9:g.6714171T= , CM000681.1:g.6714171T=	GRCh37
NC_000019.8:g.6665171T=	NCBI36
NG_009557.1:g.11492A= , LRG_27:g.11492A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.559+6A=	ENSP00000512083.1:n.559+6A=
ENST00000245907.11:c.682+6A= MANE Select	ENSP00000245907.4:n.682+6A=
ENST00000245907.10:c.682+6A=	ENSP00000245907.4:n.682+6A=
ENST00000595577.1:n.186+6A=
NM_000064.3:c.682+6A=	NP_000055.2:n.682+6A=
NM_000064.4:c.682+6A= MANE Select	NP_000055.2:n.682+6A=